Ascha Mona, Ascha Mustafa S, Tanenbaum Joseph, Bordeaux Jeremy S
Medical student at Case Western Reserve University School of Medicine, Cleveland, Ohio.
now with Department of Plastic Surgery, University Hospitals Cleveland Medical Center, Cleveland, Ohio.
JAMA Dermatol. 2017 Nov 1;153(11):1130-1136. doi: 10.1001/jamadermatol.2017.2291.
Melanoma risk factors and incidence in renal transplant recipients can inform decision making for both patients and clinicians.
To determine risk factors and characteristics of renal transplant recipients who develop melanoma.
DESIGN, SETTING, AND PARTICIPANTS: This cohort study of a large national data registry used a cohort of renal transplant recipients from the United States Renal Data System (USRDS) database from the years 2004 through 2012. Differences in baseline characteristics between those who did and did not develop melanoma were examined, and a survival analysis was performed. Patients with renal transplants who received a diagnosis of melanoma according to any inpatient or outpatient claim associated with a billing code for melanoma were included. A history of pretransplant melanoma, previous kidney transplantation, or transplantation after 2012 or before 2004 were exclusion criteria. The data analysis was conducted from 2015 to 2016.
Receipt of a renal transplant.
Incidence and risk factors for melanoma.
Of 105 174 patients (64 151 [60.7%] male; mean [SD] age, 49.6 [15.3] years) who received kidney transplants between 2004 and 2012, 488 (0.4%) had a record of melanoma after transplantation. Significant risk factors for developing melanoma vs not developing melanoma included older age among recipients (mean [SD] age, 60.5 [10.2] vs 49.7 [15.3] years; P < .001) and donors (42.6 [15.0] vs 39.2 [15.1] years; P < .001), male sex (71.5% vs 60.7%; P < .001), recipient (96.1% vs 66.5%; P < .001) and donor (92.4% vs 82.9%; P < .001) white race, less than 4 HLA mismatches (44.9% vs 37.1%; P = .001), living donors (44.7% vs 33.7%; P < .001), and sirolimus (22.3% vs 13.2%; P < .001) and cyclosporine (4.9% vs 3.2%; P = .04) therapy. Risk factors significant on survival analysis included older recipient age (hazard ratio [HR] per year, 1.06; 95% CI, 1.05-1.06; P < .001), recipient male sex (HR, 1.53; 95% CI, 1.25-1.88; P < .001), recipient white race, living donors (HR, 1.35; 95% CI, 1.11-1.64; P = .002), and sirolimus (HR, 1.54; 95% CI, 1.22-1.94; P < .001) and cyclosporine (HR, 1.93; 95% CI, 1.24-2.99; P = .004) therapy. The age-standardized relative rate of melanoma in USRDS patients compared with Surveillance, Epidemiology, and End Results patients across all years was 4.9. A Kaplan-Meier estimate of the median time to melanoma among those patients who did develop melanoma was 1.45 years (95% CI, 1.31-1.70 years).
Renal transplant recipients had greater risk of developing melanoma than the general population. We believe that the risk factors we identified can guide clinicians in providing adequate care for patients in this vulnerable group.
肾移植受者的黑色素瘤风险因素及发病率可为患者和临床医生的决策提供依据。
确定发生黑色素瘤的肾移植受者的风险因素及特征。
设计、背景和参与者:这项对大型国家数据登记处进行的队列研究使用了来自美国肾脏数据系统(USRDS)数据库中2004年至2012年的肾移植受者队列。研究了发生和未发生黑色素瘤者的基线特征差异,并进行了生存分析。纳入了根据任何与黑色素瘤计费代码相关的住院或门诊索赔被诊断为黑色素瘤的肾移植患者。移植前有黑色素瘤病史、既往肾移植史或2012年以后或2004年以前进行移植的患者为排除标准。数据分析于2015年至2016年进行。
接受肾移植。
黑色素瘤的发病率和风险因素。
在2004年至2012年接受肾移植的105174例患者(64151例[60.7%]为男性;平均[标准差]年龄49.6[15.3]岁)中,488例(0.4%)移植后有黑色素瘤记录。发生黑色素瘤与未发生黑色素瘤的显著风险因素包括受者年龄较大(平均[标准差]年龄,60.5[10.2]岁对49.7[15.3]岁;P<0.001)和供者年龄较大(42.6[15.0]岁对39.2[15.1]岁;P<0.001)、男性(71.5%对60.7%;P<0.001)、受者(96.1%对66.5%;P<0.001)和供者(92.4%对82.9%;P<0.001)为白种人、HLA错配少于4个(44.9%对37.1%;P = 0.001)、活体供者(44.7%对33.7%;P<0.001)以及使用西罗莫司(22.3%对13.2%;P<0.001)和环孢素(4.9%对3.2%;P = 0.04)治疗。生存分析中显著的风险因素包括受者年龄较大(每年风险比[HR],1.06;95%置信区间,1.05 - 1.06;P<0.001)、受者为男性(HR,1.53;95%置信区间,1.25 - 1.88;P<0.001)、受者为白种人、活体供者(HR,1.35;95%置信区间,1.11 - 1.64;P = 0.002)以及使用西罗莫司(HR,1.54;95%置信区间,1.22 - 1.94;P<0.001)和环孢素(HR,1.93;95%置信区间,1.24 - 2.99;P = 0.004)治疗。与监测、流行病学和最终结果项目的患者相比,USRDS患者各年份黑色素瘤的年龄标准化相对发病率为4.9。在确实发生黑色素瘤的患者中,黑色素瘤发生的中位时间的Kaplan - Meier估计值为1.45年(95%置信区间,1.31 - 1.70年)。
肾移植受者发生黑色素瘤的风险高于一般人群。我们认为,我们确定的风险因素可指导临床医生为这一弱势群体的患者提供充分的护理。